IP Library Granted Patent US 10,814,724
Granted Patent B2
US 10,814,724 · App. 16/388,556 · Granted Oct 27, 2020

Host cells and methods for producing isopentenol from mevalonate

Inventors: Taek Soon Lee (Berkeley, CA); Aram Kang (Richmond, CA)
Assignee: The Regents of the University of California
B60K35/00B65G69/006C07F9/091C07F9/098C08F136/08C12N9/0006C12N9/1025C12N9/1205C12N9/16C12N9/88C12P5/007C12P7/04C12Y101/01088C12Y203/0301C12Y207/01036C12Y401/01033B60K2370/173G01S2013/9314G01S2013/9317G01S2013/9323G01S2013/9324
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Quick Facts
Patent No.
US 10,814,724
App. No.
16/388,556
Granted
Oct 27, 2020
Kind
B2
Abstract

The present invention provides for a genetically modified host cell capable of producing isopentenol and/or 3-methyl-3-butenol, comprising (a) an increased expression of phosphomevalonate decarboxylase (PMD) (b) an increased expression of a phosphatase capable of converting isopentenol into 3-methyl-3-butenol, (c) optionally the genetically modified host cell does not express, or has a decreased expression of one or more of NudB, phosphomevalonate kinase (PMK), and/or PMD, and (d) optionally one or more further enzymes capable of converting isopentenol and/or 3-methyl-3-butenol into a third compound, such as isoprene.

Claims (33)

1. A genetically modified host cell capable of producing 3-methyl-3-butenol, comprising:

(a) expression of acetyl-CoA acetyltransferase (AtoB),

(b) expression of hydroxymethylglutaryl-CoA synthase (HMGS),

(c) expression of hydroxymethylglutaryl-CoA reductase (HMGR),

(d) expression of phosphomevalonate decarboxylase (PMD), wherein the PMD has an amino acid sequence having at least 90% identity with SEQ ID NO:1, and

(e) the genetically modified host cell does not express phosphomevalonate kinase (PMK);

wherein the host cell is a bacterial or fungal cell.

2. The genetically modified host cell of claim 1 , comprising wherein the PMD comprises (i) a histidine at position 74, (ii) a phenylalanine at position 145, or (iii) a histidine at position 74 and a phenylalanine at position 145, corresponding to the numbering of SEQ ID NO:1.

3. The genetically modified host cell of claim 2 , wherein the PMD comprises the following amino acid residues: (a) E at position 71, S at position 108, N at position 110, A at position 119, S at position 120, S at position 121, A at position 122, S at position 155, R at position 158, S at position 208, and D at position 302 corresponding to SEQ ID NO:1.

4. The genetically modified host cell of claim 1 , wherein the PMD has an amino acid sequence having at least 95% identity with SEQ ID NO:1.

5. The genetically modified host cell of claim 4 , wherein the PMD has an amino acid sequence having at least 99% identity with SEQ ID NO:1.

6. The genetically modified host cell of claim 1 , comprising one or more further enzymes capable of converting 3-methyl-3-butenol into a third compound.

7. The genetically modified host cell of claim 6 , wherein the third compound is isoprene.

8. The genetically modified host cell of claim 1 , wherein one or more of the PMD, AtoB, HMGS, and HMGR, are encoded on one or more nucleotide sequences which are in one or more nucleic acids which are transformed into the genetically modified host cell prior to genetic modification.

9. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is a species of the genus Escherichia, Enterobacter, Azotobacter, Erwinia, Bacillus, Pseudomonas, Klebsielia, Proteus, Salmonella, Serratia, Shigella, Rhizobia, Vitreoscilla, Paracoccus , or Clostridia.

10. The genetically modified host cell of claim 9 , wherein the genetically modified host cell is a species of the genus Escherichia.

11. The genetically modified host cell of claim 1 , wherein the genetically modified host cell is a yeast cell.

12. The genetically modified host cell of claim 11 , wherein the yeast cell is a species of the Saccharomyces genus.

13. A method for producing 3-methyl-3-butenol, comprising:

(a) providing a genetically modified host cell comprising:

(i) expression of acetyl-CoA acetyltransferase (AtoB),

(ii) expression of hydroxymethylglutaryl-CoA synthase (HMGS),

(iii) expression of hydroxymethylglutaryl-CoA reductase (HMGR),

(iv) expression of phosphomevalonate decarboxylase (PMD), wherein the PMD has an amino acid sequence having at least 90% identity with SEQ ID NO:1, and

(v) the genetically modified host cell does not express phosphomevalonate kinase (PMK), wherein the host cell is a bacterial or fungal cell; and

(b) culturing the genetically modified host cell under a condition wherein phosphomevalonate decarboxylase (PMD), acetyl-CoA acetyltransferase (AtoB), hydroxymethylglutaryl-CoA synthase (HMGS), and hydroxymethylglutaryl-CoA reductase (HMGR) are expressed.

14. The method of claim 13 , wherein the PMD comprises (i) a histidine at position 74, (ii) a phenylalanine at position 145, or (iii) a histidine at position 74 and a phenylalanine at position 145, corresponding to the numbering of SEQ ID NO:1.

15. The method of claim 13 , comprising (c) recovering the 3-methyl-3-butenol.

16. The method of claim 13 , wherein the genetically modified host cell comprises one or more further enzymes capable of converting 3-methyl-3-butenol into a third compound.

17. The method of claim 16 , comprising (c) recovering the third compound.

18. The method of claim 16 , wherein the third compound is isoprene.

19. The method of claim 18 , comprising (c) recovering the isoprene.

20. The method of claim 13 , wherein the (b) culturing step is under an anaerobic or microaerobic condition.

Assignments (2)
CONFIRMATORY LICENSE Recorded May 17, 2019
From: UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB
To: UNITED STATES DEPARTMENT OF ENERGY
Reel/Frame 049211/0982 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2019
From: LEE, TAEK SOON; KANG, ARAM
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 048931/0714 →
Continuity (4)
Continuation 15682325 · Aug 21, 2017
Continuation PCTUS2016018984 · Feb 22, 2016
Provisional Application 62119071 · Feb 20, 2015
Related Publication 20190248239A1 · Aug 15, 2019